Published July 12, 2007 | Version v1
Journal article

Microstructural characterization of oxide film formed on NiTi by anodization in acetic acid

  • 1. Department of Applied Physics, The Hong Kong Polytechnic University, Hung Hom, Kowloon (Hong Kong)
  • 2. Department of Materials and Chemical Engineering, Liaoning Institute of Technology, Jinzhou, Liaoning (China)
  • 3. Department of Industrial and Systems Engineering, The Hong Kong Polytechnic University, Hung Hom, Kowloon (Hong Kong)

Description

NiTi was galvanostatically anodized in acetic acid aiming at forming an anodic film for improving corrosion resistance. While the corrosion behavior of anodized NiTi in Hanks' solution was reported elsewhere [P. Shi, F.T. Cheng, H.C. Man, Mater. Lett., submitted for publication], the present work reports the microstructural characterization of the anodic film formed. Bright-field image of the sample cross-section captured by transmission electron microscopy (TEM) revealed an oxide film of about 20 nm thick, which was smooth and free of defects. The surface roughness R a of the film, determined by atomic force microscopy (AFM), was about 1.45 nm. Analysis by X-ray photoelectron spectroscopy (XPS) along the depth of the anodic film indicated that the oxidation state of Ti varied from +4 (corresponding to TiO2) at the surface to lower oxidation states (corresponding to Ti suboxides) beneath. A small amount of Ni in the metallic and oxidized states was also present. The Ni/Ti atomic ratio was about 0.04 at the surface of the anodic film, which was much lower than the corresponding value of 0.30 for the mechanically polished samples. Selected-area diffraction (SAD) patterns and high-resolution TEM image of the anodic film showed that the film was amorphous

Additional details

Identifiers

DOI
10.1016/j.jallcom.2006.08.020;
PII
S0925-8388(06)01034-6;

Publishing Information

Journal Title
Journal of Alloys and Compounds
Journal Volume
438
Journal Issue
1-2
Journal Page Range
p. 238-242
ISSN
0925-8388
CODEN
JALCEU

Optional Information

Copyright
Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.